FLAVONE

FLAVONE is a lipid of Polyketides (PK) class. Flavone is associated with abnormalities such as Cardiovascular Diseases, Cerebrovascular accident, DERMATITIS HERPETIFORMIS, FAMILIAL, Hyperinsulinism and Inflammatory disorder. The involved functions are known as Oxidation-Reduction, Metabolic Inhibition, Inflammation, Phosphorylation and antioxidant activity. Flavone often locates in Endothelium, Hepatic, Protoplasm, Body tissue and Extracellular. The associated genes with FLAVONE are ICAM1 gene, BCL2L1 gene, MYC gene, TP53 gene and cytochrome c''. The related lipids are Promega, Steroids and Total cholesterol. The related experimental models are Knock-out, Disease model and Animal Disease Models.

Cross Reference

Introduction

To understand associated biological information of FLAVONE, we collected biological information of abnormalities, associated pathways, cellular/molecular locations, biological functions, related genes/proteins, lipids and common seen animal/experimental models with organized paragraphs from literatures.

What diseases are associated with FLAVONE?

FLAVONE is suspected in Diabetes Mellitus, Non-Insulin-Dependent, Obesity, Chronic Disease, Disintegration, Cardiovascular Diseases, Cerebrovascular accident and other diseases in descending order of the highest number of associated sentences.

Related references are mostly published in these journals:

Disease Cross reference Weighted score Related literature
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Possible diseases from mapped MeSH terms on references

We collected disease MeSH terms mapped to the references associated with FLAVONE

MeSH term MeSH ID Detail
Lymphedema D008209 4 associated lipids
Neoplasms, Experimental D009374 10 associated lipids
Encephalitis D004660 15 associated lipids
Cystitis D003556 23 associated lipids
Neoplasm Invasiveness D009361 23 associated lipids
Adenoma D000236 40 associated lipids
Leukemia P388 D007941 43 associated lipids
Lupus Erythematosus, Systemic D008180 43 associated lipids
Osteosarcoma D012516 50 associated lipids
Asthma D001249 52 associated lipids
Weight Loss D015431 56 associated lipids
Dermatitis, Contact D003877 59 associated lipids
Pain D010146 64 associated lipids
Mammary Neoplasms, Experimental D008325 67 associated lipids
Melanoma D008545 69 associated lipids
Carcinoma, Non-Small-Cell Lung D002289 72 associated lipids
Hyperlipidemias D006949 73 associated lipids
Stomach Ulcer D013276 75 associated lipids
Pancreatic Neoplasms D010190 77 associated lipids
Diabetes Mellitus, Experimental D003921 85 associated lipids
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PubChem Associated disorders and diseases

What pathways are associated with FLAVONE

There are no associated biomedical information in the current reference collection.

PubChem Biomolecular Interactions and Pathways

Link to PubChem Biomolecular Interactions and Pathways

What cellular locations are associated with FLAVONE?

Related references are published most in these journals:

Location Cross reference Weighted score Related literatures
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What functions are associated with FLAVONE?


Related references are published most in these journals:

Function Cross reference Weighted score Related literatures

What lipids are associated with FLAVONE?

Related references are published most in these journals:

Lipid concept Cross reference Weighted score Related literatures
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What genes are associated with FLAVONE?

Related references are published most in these journals:


Gene Cross reference Weighted score Related literatures

What common seen animal models are associated with FLAVONE?

Knock-out

Knock-out are used in the study 'MATE2 mediates vacuolar sequestration of flavonoid glycosides and glycoside malonates in Medicago truncatula.' (Zhao J et al., 2011) and Knock-out are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Disease model

Disease model are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Animal Disease Models

Animal Disease Models are used in the study 'How can research on plants contribute to promoting human health?' (Martin C et al., 2011).

Related references are published most in these journals:

Model Cross reference Weighted score Related literatures
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NCBI Entrez Crosslinks

All references with FLAVONE

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Per page 10 20 50 100 | Total 1492
Authors Title Published Journal PubMed Link
Zhao L et al. The antitumour activity of 5,6-dimethylxanthenone-4-acetic acid (DMXAA) in TNF receptor-1 knockout mice. 2002 Br. J. Cancer pmid:12177785
Hori K et al. A novel combretastatin A-4 derivative, AC7700, strongly stanches tumour blood flow and inhibits growth of tumours developing in various tissues and organs. 2002 Br. J. Cancer pmid:12085211
Ching LM et al. Induction of endothelial cell apoptosis by the antivascular agent 5,6-Dimethylxanthenone-4-acetic acid. 2002 Br. J. Cancer pmid:12085190
Jacobson KA et al. Interactions of flavones and other phytochemicals with adenosine receptors. 2002 Adv. Exp. Med. Biol. pmid:12083460
Kuffel MJ et al. Activation of the antitumor agent aminoflavone (NSC 686288) is mediated by induction of tumor cell cytochrome P450 1A1/1A2. 2002 Mol. Pharmacol. pmid:12065765
Hadjokas NE et al. Arginine to lysine 108 substitution in recombinant CYP1A2 abolishes methoxyresorufin metabolism in lymphoblastoid cells. 2002 Br. J. Pharmacol. pmid:12023936
Lin YM et al. Chalcones and flavonoids as anti-tuberculosis agents. 2002 Bioorg. Med. Chem. pmid:12057669
Han DH et al. Relationship between estrogen receptor-binding and estrogenic activities of environmental estrogens and suppression by flavonoids. 2002 Biosci. Biotechnol. Biochem. pmid:12224631
Shimizu E and Ogata Y Activation of bone sialoprotein gene transcription by flavonoids is mediated through an inverted CCAAT box in ROS 17/2.8 cells. 2002 J. Cell. Biochem. pmid:12112014
Matsui T et al. Luteolin, a flavone, does not suppress postprandial glucose absorption through an inhibition of alpha-glucosidase action. 2002 Biosci. Biotechnol. Biochem. pmid:12005074
Cai H et al. A straightforward means of coupling preparative high-performance liquid chromatography and mass spectrometry. 2002 Rapid Commun. Mass Spectrom. pmid:11870892
Kahnberg P et al. Refinement and evaluation of a pharmacophore model for flavone derivatives binding to the benzodiazepine site of the GABA(A) receptor. 2002 J. Med. Chem. pmid:12213060
Vrielynck L et al. Self-modelling analysis applied to nanosecond transient absorption spectroscopy of flavone: an aid to elucidate and characterise reaction intermediates. 2002 Spectrochim Acta A Mol Biomol Spectrosc pmid:12396046
Blatt CT et al. Cytotoxic flavonoids from the stem bark of Lonchocarpus aff. fluvialis. 2002 Phytother Res pmid:12112286
Choi J et al. Flavones from Scutellaria baicalensis Georgi attenuate apoptosis and protein oxidation in neuronal cell lines. 2002 Biochim. Biophys. Acta pmid:12090934
Rawel HM et al. Interactions of different phenolic acids and flavonoids with soy proteins. 2002 Int. J. Biol. Macromol. pmid:12063116
Fang J and Beattie DS Novel FMN-containing rotenone-insensitive NADH dehydrogenase from Trypanosoma brucei mitochondria: isolation and characterization. 2002 Biochemistry pmid:11863445
López-Lázaro M Flavonoids as anticancer agents: structure-activity relationship study. 2002 Curr Med Chem Anticancer Agents pmid:12678721
Cook SA and Shiemke AK Evidence that a type-2 NADH:quinone oxidoreductase mediates electron transfer to particulate methane monooxygenase in methylococcus capsulatus. 2002 Arch. Biochem. Biophys. pmid:11811946
Guz NR et al. Flavonolignan and flavone inhibitors of a Staphylococcus aureus multidrug resistance pump: structure-activity relationships. 2001 J. Med. Chem. pmid:11170636
Duportail G et al. Neutral fluorescence probe with strong ratiometric response to surface charge of phospholipid membranes. 2001 FEBS Lett. pmid:11718715
Krakauer T et al. The flavonoid baicalin inhibits superantigen-induced inflammatory cytokines and chemokines. 2001 FEBS Lett. pmid:11434925
Fabre N et al. Determination of flavone, flavonol, and flavanone aglycones by negative ion liquid chromatography electrospray ion trap mass spectrometry. 2001 J. Am. Soc. Mass Spectrom. pmid:11401161
Kanwar JR et al. Vascular attack by 5,6-dimethylxanthenone-4-acetic acid combined with B7.1 (CD80)-mediated immunotherapy overcomes immune resistance and leads to the eradication of large tumors and multiple tumor foci. 2001 Cancer Res. pmid:11280751
Galietta LJ et al. Novel CFTR chloride channel activators identified by screening of combinatorial libraries based on flavone and benzoquinolizinium lead compounds. 2001 J. Biol. Chem. pmid:11262417
Goto S and Handa S Antithrombotic effects of flavonoid. 2001 Circulation pmid:11157735
Tanaka S et al. Influence of natural and synthetic compounds on cell surface expression of cell adhesion molecules, ICAM-1 and VCAM-1. 2001 Planta Med. pmid:11301853
Summanen J et al. Effects of simple aromatic compounds and flavonoids on Ca2+ fluxes in rat pituitary GH(4)C(1) cells. 2001 Eur. J. Pharmacol. pmid:11239912
Fang H et al. Structure-activity relationships for a large diverse set of natural, synthetic, and environmental estrogens. 2001 Chem. Res. Toxicol. pmid:11258977
Lebeau J et al. Beneficial effects of different flavonoids, on functional recovery after ischemia and reperfusion in isolated rat heart. 2001 Bioorg. Med. Chem. Lett. pmid:11140725
Park BK et al. Inhibition of TPA-induced cyclooxygenase-2 expression and skin inflammation in mice by wogonin, a plant flavone from Scutellaria radix. 2001 Eur. J. Pharmacol. pmid:11502282
Rajendran NN et al. Modulation by insulin rather than blood glucose of the pain threshold in acute physiological and flavone induced antinociception in mice. 2001 Indian J. Exp. Biol. pmid:11883508
Chi YS et al. Effect of wogonin, a plant flavone from Scutellaria radix, on the suppression of cyclooxygenase-2 and the induction of inducible nitric oxide synthase in lipopolysaccharide-treated RAW 264.7 cells. 2001 Biochem. Pharmacol. pmid:11322923
Andrade-Cetto A and Wiedenfeld H Hypoglycemic effect of Cecropia obtusifolia on streptozotocin diabetic rats. 2001 J Ethnopharmacol pmid:11694359
Chung MI et al. Synthesis, antiplatelet and vasorelaxing effects of monooxygenated flavones and flavonoxypropanolamines. 2001 J. Pharm. Pharmacol. pmid:11804390
Kestell P et al. Measurement of plasma 5-hydroxyindoleacetic acid as a possible clinical surrogate marker for the action of antivascular agents. 2001 Clin. Chim. Acta pmid:11718691
Hirvonen T et al. Flavonol and flavone intake and the risk of cancer in male smokers (Finland). 2001 Cancer Causes Control pmid:11714106
D'arc Felicio J et al. Biflavonoids from Ouratea multiflora. 2001 Fitoterapia pmid:11395278
Lim SS et al. Synthesis of flavonoids and their effects on aldose reductase and sorbitol accumulation in streptozotocin-induced diabetic rat tissues. 2001 J. Pharm. Pharmacol. pmid:11370705
Recanatini M et al. A new class of nonsteroidal aromatase inhibitors: design and synthesis of chromone and xanthone derivatives and inhibition of the P450 enzymes aromatase and 17 alpha-hydroxylase/C17,20-lyase. 2001 J. Med. Chem. pmid:11262078
Marder M et al. Molecular modeling and QSAR analysis of the interaction of flavone derivatives with the benzodiazepine binding site of the GABA(A) receptor complex. 2001 Bioorg. Med. Chem. pmid:11249125
Klein M et al. The ABC-like vacuolar transporter for rye mesophyll flavone glucuronides is not species-specific. 2001 Phytochemistry pmid:11219807
Manthey JA et al. Biological properties of citrus flavonoids pertaining to cancer and inflammation. 2001 Curr. Med. Chem. pmid:11172671
Dertinger SD et al. Aryl hydrocarbon receptor signaling plays a significant role in mediating benzo[a]pyrene- and cigarette smoke condensate-induced cytogenetic damage in vivo. 2001 Carcinogenesis pmid:11159756
Hirvonen T et al. Intake of flavonols and flavones and risk of coronary heart disease in male smokers. 2001 Epidemiology pmid:11138821
Lee SE et al. Inhibitory effects of naturally occurring compounds on aflatoxin B(1) biotransformation. 2001 J. Agric. Food Chem. pmid:11714299
Schrag ML and Wienkers LC Covalent alteration of the CYP3A4 active site: evidence for multiple substrate binding domains. 2001 Arch. Biochem. Biophys. pmid:11414684
Huang X et al. 3D-QSAR model of flavonoids binding at benzodiazepine site in GABAA receptors. 2001 J. Med. Chem. pmid:11384234
Velázquez I and Pardo JP Kinetic characterization of the rotenone-insensitive internal NADH: ubiquinone oxidoreductase of mitochondria from Saccharomyces cerevisiae. 2001 Arch. Biochem. Biophys. pmid:11370674
Rossi M et al. Molecular structure and activity toward DNA of baicalein, a flavone constituent of the Asian herbal medicine "Sho-saiko-to". 2001 J. Nat. Prod. pmid:11170661